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The Cambridge Group Ltd
1175 Post Road East
Westport CT 06880
800-525-3396
Web: www.cambridgegroup.com

Long - term consulting engagement, 40 hrs/week

Length: Initial term: 5 months + extension
Rate: $50.00 - $60.00 per hour ($104,000 - $124,800 annualized)

Provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials. Employ standardized programs where applicable. Provide input into planning documents such as protocol, validation plan, and report analysis plan. Provide outputs for clinical study reports, integrated summaries and electronic submissions. Help respond to health authority inquiries for submitted dossiers. Establish and maintain sound working relationship and effective communications within biostatistics and statistical reporting and clinical research.

Requirements:

  • 1-2 years of Analytical experience. BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s).
  • Intermediate SAS programming skills, with 2-5 years experience in a medical setting, preferably working with clinical trial data.
  • Good understanding of clinical trial practices, procedures and methodologies.
  • Good verbal and written communication skills.
  • Good interpersonal and organizational skills.
  • Attention to detail and correctness.
  • Working knowledge of office tools.
  • MS in Statistics a plus.
  • Contact:
    The Cambridge Group Ltd
    Spiro Michas
    Email:
    800 295-0332



    Julie Youmans-Smith
    SW Jules, Inc.
    8760-A Research Blvd., #264
    Austin, TX 78758
    Phone: 1-501-723-8492
    A NATIONAL PHARMACEUTICAL, HIGH TECH AND EXECUTIVE RECRUITMENT CORPORATION
    PROPELLING RELATIONSHIPS
    Email:
    Web: WWW.SWJULES.COM

    SENIOR STATISTICIAN - TEXAS Reference job code T-BIOSR-SCONSIG-1

    SW JULES, INC. has an established client looking for senior biostatisticians. To be considered you must have experience within Biotech/Pharmaceutical or CRO company with Phase I-IV Clinical Trial Analysis and reporting to the FDA.

    QUALIFICATIONS

  • Ph.D. in Statistics or Biostatistics and 6 years relevant statistical experience in the clinical trials environment.
  • OR a MS in Statistics or Biostatistics and 10 years relevant statistical experience in the clinical trials environment
  • Excellent written and oral communication skills including grammatical/technical writing skills
  • Excellent attention and accuracy with details
  • Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials
  • Strong organizational skills
  • Supervisory Skills A MUST
  • To receive additional information on this position please Send resume as a MS WORD attachment to
    Julie Youmans-Smith
    Email:

    SENIOR STATISTICIAN - SOUTHERN CALIFORNIA Reference job code C-BIOSR-SCONSIG-1

    SW JULES, INC. has an established client looking for senior biostatisticians. To be considered you must have experience within Biotech/Pharmaceutical or CRO company with Phase I-IV Clinical Trial Analysis and reporting to the FDA.

    QUALIFICATIONS

  • Ph.D. in Statistics or Biostatistics and 6 years relevant statistical experience in the clinical trials environment.
  • OR a MS in Statistics or Biostatistics and 10 years relevant statistical experience in the clinical trials environment
  • Excellent written and oral communication skills including grammatical/technical writing skills
  • Excellent attention and accuracy with details
  • Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials
  • Strong organizational skills
  • Supervisory Skills A MUST
  • To receive additional information on this position please Send resume as a MS WORD attachment to
    Julie Youmans-Smith
    Email:

    SENIOR STATISTICIAN - PENNSYLVANIA Reference job code P-BIOSR-SCONSIG-1

    SW JULES, INC. has an established client looking for senior biostatisticians. To be considered you must have experience within Biotech/Pharmaceutical or CRO company with Phase I-IV Clinical Trial Analysis and reporting to the FDA.

    QUALIFICATIONS

  • Ph.D. in Statistics or Biostatistics and 6 years relevant statistical experience in the clinical trials environment.
  • OR a MS in Statistics or Biostatistics and 10 years relevant statistical experience in the clinical trials environment
  • Excellent written and oral communication skills including grammatical/technical writing skills
  • Excellent attention and accuracy with details
  • Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials
  • Strong organizational skills
  • Supervisory Skills A MUST
  • To receive additional information on this position please Send resume as a MS WORD attachment to
    Julie Youmans-Smith
    Email:


    Professional Resources, Inc.
    Ted Phillips
    4 Daniels Farm Rd.
    Suite #325
    Trumbull, CT 06611
    Phone: 203-268-9696
    Email:
    Web: www.pricareers.com

    Contract SAS Programmer - CT

    Duration: 1 Year
    BASIC PURPOSE: Under general direction, support clinical drug development process by writing standard validated programs/macros/procedures which support the monitoring and reporting activities associated with clinical trials. Designs structured diagrams based on user needs/requirements and works with other departments where necessary to produce SAS programs or fully integrated applications which will enhance performance of the users. Assures quality by establishing and administering of guidelines and standards for coding, documentation and validation of SAS and application programs/macros/procedures and maintaining libraries of SAS programs and application code written to support clinical drug development. Assist in the training of Medical Department personnel in the use and application of computer system tools to facilitate efficient, quality-orientated performance of their duties.

    BASIC REPOSIBILITIES/ESSENTIAL FUNCTIONS;

  • Establish standardized data displays and standard edit checks to support clinical trial integrated reports, INDs, PLAs, NDAs and DIRs. Responsible for the proper coding, documentation and validation of programs/macros/procedures to produce the standardized data displays.
  • Analyze requests for application programming support and work with other departments to decide upon the appropriate computer tool to use. Where necessary, produces/transforms users requirements/structured diagrams into SAS code, or macros/procedures within application software creating a fully documented, validated application which can be used by the requester and others to satisfy their needs.
  • Establish and maintain libraries of fully documented and validated applications programs/macros/procedures which are used and recycled whenever possible to support the monitoring and reporting of data from clinical trials
  • Establish guidelines and standard operating procedures for the coding, documentation and validation of applications programs/macros/procedures which support monitoring and reporting of clinical trial data.
  • Ensure proper and consistent implementation and maintenance of guidelines and standards within the data management group.

  • Contract SAS Programmer - MA

    Duration: 1 Year
    Job Description/Key Duties:
  • The Senior SAS Programmer is responsible for the programming of graphs, tables and listings for statistical and clinical report writing and clinical trial database validation.
  • Candidate will need to posses a high proficiency in base SAS, SAS/Graph, SAS/Stat and SAS Macro language. Familiarity with medical terminology, physiology, anatomy and standardized medical coding dictionaries.
  • Strong interpersonal skills, including both written and oral communications. Ability to work in a team environment and the ability to adapt to a fast moving environment. Minimum of a BS/BA in Computer Science, Mathematics, Statistics or other related field. MS in Biostatistics is preferred.

  • SAS Contract Programmer - CA

    Duration: 1+ Year
    Job: Responsible for performing analyses on clinical trial data, including listings, tabulations, graphical summaries and formal statistical estimates and tests. Must be able to assess quality of analysis data, perform cross study analyses and be able to create and use/write SAS macros to automate all of the above functions. Candidate needs be able to design and create analysis data bases for electronic NDA submission. Must have a thorough knowledge of study design and NDA submission requirements. Candidate will be responsible for mentoring junior programmers in the areas of SAS coding and study analysis.

    A Bachelor's or Master's degree in Statistics or Computer Sciences with 5 years of industry experience is required. Good written and oral communication skills are a must. An exceptional knowledge in SAS/Base, SAS/Macro, SAS/Graph, SAS/Stat and the ability to write maintainable, supportable and well-documented SAS code is essential.


    Contact:
    Ted Phillips
    President
    PRI, Inc.
    4 Daniels Farm Rd.
    Suite #325
    Trumbull, CT 06611
    203-268-9696
    Email:
    www.pricareers.com



    Analytic Recruiting Inc.
    12 East 41st Street, 9th Floor
    New York, NY 10017
    Phone: 212 545-8511
    Fax: 212-545-8520
    Website: www.analyticrecruiting.com
    Email:

    Claims Statistical Analyst – North Bay, CA (JV294)

    California insurance company seeks Analyst to support the analytical needs of regional directors and product managers. Use statistical methodologies on varied data sources to identify key metrics, perform analysis to deepen the business understanding (preparing and leading workshops, etc.), build statistical models, forecast from those models, communicate results to non-technical personnel and recommend actionable changes to the organization.

    Requirements:

  • B.S. Statistics or similar. Graduate degree preferred.
  • 3+ years experience as a data analyst, insurance or financial services experience preferred.
  • Experience in exploratory data analysis, multivariate statistics, time-series analysis, generalized linear regression, logistic regression, factor analysis, hypothesis testing, etc.
  • Knowledge of one or more statistical packages: SAS, S/S+/R, SPSS, or similar package. Knowledge of DB2 and MS SQL Server, Microsoft Excel. Powerpoint Excel experience that includes generating Pivot Tables, writing macros using VBA, querying external data sources.
  • Experience with any major integrated Business Intelligence platform, e.g. Business Object, MicroStrategies, Cognos, etc.
  • Experience with automated model building and data mining.
  • Knowledge of data warehousing concepts.
  • Strong communication and networking skills. Ability to communicate results to non-technical audiences.
  • Salary $75-100k.

    Refer to Job#12611-Sconsig and email MS Word attached resume to
    Jamie Voronkov
    Email:
    register online at www.analyticrecruiting.com choosing Jamie Voronkov as your recruiter contact.

    Senior Media Analyst - VA (JV293)

    Virginia based Direct Marketing Agency is looking for a Senior Media Analyst to join their Analytic Development group.

    Responsibilities:

  • Co-develop media analytics capabilities presentation
  • Participate in business development effort, including travel as needed
  • Identify software and data requirements for media analytics
  • Cross-train other analysts
  • Work with clients to optimize their media investments:

  • Identify target metric(s)
  • Assess historic media data usefulness
  • Aid in designing experiments to isolate media effects
  • Develop media mix models and optimal solutions
  • Co-develop simulation tools that enable "what-if" scenario interaction
  • Conduct full range of direct marketing analytics, including design of experiments, campaign tracking, profiling, segmentation and predictive modeling

    Qualifications:

  • Graduate degree in Statistics/Economics
  • SAS proficiency (5+ yrs experience)
  • 5+ yrs experience in media analysis and modeling
  • Strong written and verbal communication skills
  • Ability to convey technical concepts to marketing and advertising professionals
  • Salary to 120k

    Refer to Job#12616-Sconsig and email MS Word attached resume to
    Jamie Voronkov
    Email:
    register online at www.analyticrecruiting.com choosing Jamie Voronkov as your recruiter contact.

    Business Analyst - TX (HF55)

    Work on partnerships businesses for Dallas area financial services M&A.

    Responsibilities include:

  • Product development and pricing/optimization strategy across several existing partnerships
  • Establish pricing and credit policies for new potential partners.
  • Develop and manage economic models to help understand credit losses and economics
  • Conduct analysis to understand competitive product offerings and pricing in the indirect marketplace
  • Assemble comprehensive analyses to address business problems, build case for policy changes that improve the credit loss and economic performance of the business
  • Develop credit policies, work with project managers to implement credit policies, monitor results of credit policies
  • Qualifications:

  • BA/BS in a quantitative field
  • Strong analytical and strategic thinking skills
  • Good organization and multi-tasking ability
  • Solid communication and presentation skills
  • Preferred

  • Consulting background ins a plus
  • Previous experience in pricing or optimization
  • Prior experience in risk management
  • Auto Industry Experience
  • Direct Mail marketing or risk analysis experience
  • Fluency in pulling and manipulation data using SAS and SQL server
  • Salary $65-80k + bonus.

    Refer to Job#12589-Sconsig and email MS Word attached resume to
    Howard Fishman
    Email:
    register online at www.analyticrecruiting.com choosing Howard as your recruiter contact.


    Customer Management Professionals - CT (HF53)

    Connecticut financial services company has several openings for professionals to leverage business, marketing, direct marketing and analytic skills to measurably enhance customer performance.

    Responsibilities entail:

  • Championing retention, acquisition, and cross sell projects.
  • Developing and testing strategic initiatives to improve all customer contacts points (including mail, e-commerce, inbound/outbound telemarketing, and point of sale).
  • Financial/marketing reporting and forecasting to establish customer and program baselines, and to measurably/positively impact those baselines.
  • Managing analytic projects to develop actionable direct value-added products (for example, customer and store focused statistical models and product affinity analyses).
  • Train and coach marketing teams in cutting edge direct marketing concepts, testing and implementation. Provide strategic-level direct marketing consulting support.
  • Requirements

  • 5 to 7-plus years of progressive experience in direct marketing with at least3 years in a retail and/or financial (esp. Bank Card) environment.
  • Significant experience in the creative, production, and analytic elements of direct marketing.
  • An effective presenter, facilitator, and influencer
  • Proven ability to support multiple competing projects/tasks.
  • Understanding of privacy issues & legal compliance in the direct marketing and financial environment.
  • Extensive familiarity of SAS and/or SQL. Thorough knowledge of acquisition, retention, and cross sell direct mail concepts. Deep understanding of financial and marketing reporting and forecasting.
  • Four Year Degree in a Relevant Field required.
  • Experience interacting in an international environment.
  • MBA. GB Certified
  • Salary $51-96k + bonus.

    Refer to Job#12580-Sconsig and email MS Word attached resume to
    Howard Fishman
    Email:
    register online at www.analyticrecruiting.com choosing Howard as your recruiter contact.


    SAS Application Developer II - Bloomfield, CT

    Contact:
    Ron Stoloff
    Senior Staffing Consultant
    CIGNA
    1601 Chestnut Street , TL06k
    Philadelphia, PA 19192
    215-761-3715
    Email:

    Click here to read job description and requirements (PDF format)



    The Cambridge Group Ltd
    1175 Post Road East
    Westport CT 06880
    800-525-3396
    Web: www.cambridgegroup.com

    SAS Programmer - 1447

    JoiN this CRO for a senior statistical programmer role. You will report to the manager, statistical programming. You will be responsible for leading the development and maintenance of analysis programs to support clients' drug development projects, leading the communication of technical issues with lead client staff and internal team staff, and contributing to internal technological advances. The Primary Responsibilities will be as follows:
  • Leads the implementation of data listing, summary, and graphs for inclusion in new drug applications (NDAs)
  • Contributes to the development of and training on Standard Operating Procedures (SOPs)
  • Develops software for standard operating systems
  • Provides technical consult on clients’ needs to Operations staff
  • Troubleshoots as required for staff and clients regarding specific programming concerns
  • Reviews listing, summary, graph, and tabulation specifications
  • Provides secondary review of statistical programming deliverables
  • Develops standard programming procedures
  • Supports programming needs within Operations
  • Other duties as assigned
  • Education: BA or BS in computer science, statistics, mathematics, or information technology.

    Experience:

    At least two years programming experience with demonstrated leadership skills at a CRO or a Pharmaceutical company with clinical trial experience. Extensive knowledge of SAS and knowledge of C, C++, Pascal, or other high-level 3rd or 4th generation languages is preferable. Exposure to pharmaceutical, biotechnology or device industry highly desired. Equivalent combination of education and work experience may be substituted.

    Salary/Benefits: Salary depending on experience, full benefits.

    Contact:
    Bonnie Grettler
    800 525-3396
    Fax: 202 226-3856
    Email:



    The Cambridge Group Ltd
    1175 Post Road East
    Westport CT 06880
    800-525-3396
    Web: www.cambridgegroup.com

    Project Leader SAS Programming - 1838 - New Jersey

    NJ Pharmaceutical has 4 openings for candidates with strong SAS programming skills to function as Project Leaders. You will support Phase I-III clinical rials and be responsible for developing reporting databases and derived analysis datasets, providing outputs for the Clinical Study Report, Clinical Summary of Safety and electronic files for submission to the FDA and global regulatory agencies, and oversee the programming activities of up to 4 programmers.

    Qualified applicants will possess 6 years of programming experience, with at least 3 of those years working with clinical trial data. A strong knowledge of SAS report writing and SAS Macro is also needed and experience with SAS/STAT, SAS/GRAPH, SAS/CONNECT is considered a plus. You must have good communication skills in order to effectively participate in a cross-functional team environment. Computing environment is UNIX and LAN.

    Salary/Benefits: Salary depending on experience, full benefits.

    Contact
    Traci Palmer
    800 525-3396
    Fax: 202 226-3856
    Email: